JP4805416B1 - Optical information analysis apparatus and optical information analysis method - Google Patents

Abstract

By providing a light receiving part that receives transmitted light at a position directly opposite the irradiation part and adjusting the position of the sample flow relative to the measurement region in the flow path, the sensitivity of the received transmitted light is increased and variation is achieved. Provided are an optical information analysis apparatus and an optical information analysis method capable of obtaining optical information of a specimen with a small amount.
The optical information analysis apparatus 10 includes an irradiation unit 30 that irradiates the specimen S with the irradiation light L0, a transmitted light receiving unit 50 that receives the transmitted light L1 and detects it as a transmitted light signal SG1, and side scattered light and fluorescence L2. A scattering / fluorescence light receiving unit 60 that receives and detects the scattered / fluorescent signal SG2, and a nozzle position adjusting mechanism 80 that adjusts the position of the tip 15a of the introduction nozzle 15 according to the transmitted light receiving unit 50 and the irradiation unit 30; An analysis unit 90 that measures light information of the specimen S and analyzes the specimen S based on the detected transmitted light signal SG1 and the scattered / fluorescent signal SG2.
[Selection] Figure 1

Description

  The present invention relates to an optical information analysis apparatus and an optical information analysis method. In particular, the present invention relates to an optical information analysis apparatus and an optical information analysis method for measuring optical information of a specimen by irradiating the specimen, which is a measurement target, dispersed in a liquid flowing in a flow path with irradiation light.

  A liquid containing the stained biological particles (test specimen: specimen) is allowed to flow through the flow path of the flow path forming member (flow cell), and the light irradiated from the illumination section (irradiation section) is applied to the biological particles. In addition, a device (flow cytometer, cell sorter) that detects scattered light and fluorescence from the biological particle by a detection unit (light receiving unit) and obtains biological information of the biological particle has been proposed (for example, Patent Document 1).

  Conventionally, in the apparatus as described above, the sample flow, which is the flow of the liquid flowing through the flow channel in the flow cell, is adjusted to flow in the vicinity of the center of the flow channel by being wrapped in the sheath flow. The optical axis and the focal point of the optical system of the part are fixed in accordance with the center of the flow path in the flow cell on a plane substantially orthogonal to the sample flow. In addition, the irradiation unit irradiates the irradiation light condensed on the sample flow and receives scattered light and fluorescence from the specimen, thereby obtaining highly sensitive scattered light and fluorescence and obtaining light information on the specimen with little variation. Therefore, the position of the optical axis of the irradiation unit can be optimally adjusted with respect to the sample flow while actually irradiating the sample flow with the irradiation light and checking the optical information.

Japanese Patent No. 3899925

  However, in the conventional apparatus as described above, when the sample flow passes a position deviated from the center of the flow path in the flow cell, the optical axis of the irradiation unit is aligned with the sample flow. There has been a problem that the optical axis does not cross the sample flow and the optical axis of the irradiation section. For this reason, the light receiving unit is configured to receive a wide range of light, and as a result, the sensitivity of the scattered light and fluorescence detected is reduced, and the optical information of the obtained specimen varies.

  In addition, the optical axis of the irradiation unit can only be adjusted while the sample flow is actually created by flowing a liquid through the flow channel in the flow cell, and the optical axis of the irradiation unit cannot be easily adjusted. There was also.

  Accordingly, the present invention has been made to solve the above-described problems. A light receiving portion for receiving transmitted light is provided at a position facing the irradiation portion, and the sample flow is measured with respect to the measurement region in the flow path. The optical information analyzing apparatus and the optical information analyzing method capable of increasing the sensitivity of the transmitted light received by the light receiving unit and obtaining the optical information of the sample with little variation by relatively adjusting the position of the light receiving unit. With the goal.

の関係式を満たすことを特徴とする。 The following invention is provided to solve the above-mentioned conventional problems.
The optical information analysis apparatus according to the first aspect of the present invention irradiates the specimen as the measurement target dispersed in the liquid flowing in the flow path with the single-mode irradiation light, thereby providing optical information on the specimen. A flow cell having the flow path, an introduction nozzle for introducing the liquid into the flow path of the flow cell, and the irradiation light to the liquid flowing through the flow path of the flow cell. An irradiating unit that irradiates, and a transmission provided at a position facing the irradiating unit via the flow cell that receives the transmitted light of the liquid by the irradiated light irradiated from the irradiating unit and detects it as a transmitted light signal. A light receiving unit, and an analysis unit that measures and analyzes the optical information of the specimen based on the transmitted light signal detected by the transmitted light receiving unit,
The transmitted light receiving unit includes an optical fiber disposed so that a light receiving surface substantially orthogonal to an optical axis faces the irradiation unit, and a center of the light receiving surface substantially coincides with an optical axis of the irradiation unit,
The core diameter of the optical fiber is d, the cladding diameter of the optical fiber is d ′, the irradiation diameter of the irradiation light irradiated from the irradiation unit on the light receiving surface of the optical fiber is D , and the optical fiber When the irradiation outer diameter of the irradiation light irradiated from the irradiation unit on the light receiving surface is D ′,

The above relational expression is satisfied.

Here, the single mode is a single transverse mode, and a Gaussian distribution is desirable. However, the intensity distribution may be made partially uniform or the beam shape may be elliptical according to the measurement target. Absent. It is desirable that the irradiation light intensity is constant. The irradiation diameter D is a beam diameter, which is a diameter having an intensity of 1 / e ² (= 13.5%) of the beam center intensity.
The introduction nozzle does not have to have a shape in which the tip portion protrudes, and it is sufficient if a hole through which the liquid passes is formed.
Transmitted light refers to light received by the transmitted light receiving unit, such as light that has passed through the liquid in which the specimen is dispersed, light that has passed through the specimen, and light that has been reflected, scattered, and diffracted by the specimen. The transmitted light signal is a signal obtained by converting the transmitted light into an electrical signal. In an arbitrary region that receives transmitted light, the light is received, and the amount of received light (transmitted light signal) varies during sample measurement. The peak, width, area, etc. of the fluctuation are called optical information.

In here, the core diameter d is equivalent to JIS C 6820 (optical fiber rules).

  Here, the cladding diameter d ′ conforms to JIS C 6820 (General rules for optical fibers). Further, the irradiation outer diameter D ′ refers to a diameter that is 5% of the beam center intensity.

The optical information analysis apparatus according to the second aspect of the present invention is the optical information analysis apparatus according to the first aspect of the present invention, wherein the flow path is determined based on the configuration of the irradiation unit and the transmitted light receiving unit. An adjustment unit is further provided that adjusts the position of the sample flow by the liquid in the flow channel relative to the measurement region.

  Here, the sample flow is a flow of the liquid containing the specimen when the liquid is flowed through the flow path of the flow cell. The center of the sample flow is a center position within the passage range of the sample flow on a plane orthogonal to the flow direction of the sample flow. Further, the position of the sample flow in the flow path is a position through which the center of the sample flow passes on a surface in the flow path that is orthogonal to the flow direction of the sample flow.

The optical information analysis apparatus according to the third aspect of the present invention is the optical information analysis apparatus according to the first or second aspect of the present invention, wherein the side of the specimen by the irradiation light irradiated from the irradiation unit is provided. A scattered / fluorescent light receiving unit that receives scattered light and / or fluorescence and detects it as a scattered / fluorescent signal, and is provided at a position where the optical axis intersects the optical axis of the irradiated unit and does not face the irradiated unit. It is characterized by further providing at least one.

The optical information analysis apparatus according to the fourth aspect of the present invention is the optical information analysis apparatus according to the third aspect of the present invention, wherein the scattering / fluorescence light receiving unit has a light receiving surface substantially orthogonal to the optical axis, An optical fiber is provided so as not to face the irradiation unit.

An optical information analysis apparatus according to a fifth aspect of the present invention is the optical information analysis apparatus according to the third or fourth aspect of the present invention described above, wherein the optical axis of the irradiating unit and the optical axis of the scattering / fluorescence receiving unit. Are substantially orthogonal to each other.

An optical information analysis apparatus according to a sixth aspect of the present invention is the optical information analysis apparatus according to any one of the second to fifth aspects of the present invention, wherein the approximate center of the sample flow is the measurement region. The position of the sample flow in the flow path is relatively adjusted so as to pass through substantially the center.
Here, the measurement region is determined based on the diameter of the irradiation light irradiated from the irradiation unit in the flow path and the light receiving region of the transmitted light receiving unit and the scattering / fluorescence receiving unit. In addition, the approximate center of the measurement region refers to the approximate center position of the length of the optical axis in the measurement region on the optical axis of the irradiation unit and the transmitted light receiving unit that are substantially coincident with each other.

An optical information analysis apparatus according to a seventh aspect of the present invention is the optical information analysis apparatus according to any one of the third to fifth aspects of the present invention, wherein the adjustment unit has an approximate center of the sample flow. , Crossing the optical axis of the desired at least one of the scattering / fluorescence light receiving unit from the approximate center of the measurement region, and passing through a position away from the crossed scattering / fluorescence light receiving unit. The position of the sample stream is relatively adjusted.

An optical information analysis device according to an eighth aspect of the present invention is the optical information analysis device according to any one of the second to seventh aspects of the present invention described above, wherein the adjustment unit is arranged in the flow path of the flow cell. A nozzle position adjusting mechanism that adjusts the position of the leading end of the introduction nozzle, and the position of the leading end of the introducing nozzle in the flow path of the flow cell is adjusted by the nozzle position adjusting mechanism. Is adjusted with respect to the measurement region.

An optical information analysis device according to a ninth aspect of the present invention is the optical information analysis device according to any one of the second to seventh aspects of the present invention described above, wherein the adjustment unit is mounted with the introduction nozzle. Adjusting the position of the tip of the introduction nozzle in the flow path of the flow cell by being fixed to the flow cell, comprising a plurality of offset jigs having different positions of the tip of the introduction nozzle, and a plurality of the offsets Adjusting the position of the tip of the introduction nozzle in the flow path with the optimum offset jig selected from among the jigs so that the desired sample flow position is obtained with respect to the measurement region It is characterized by.

An optical information analysis device according to a tenth aspect of the present invention is the optical information analysis device according to any one of the first to ninth aspects of the present invention, wherein the irradiation unit propagates the irradiation light. It is characterized by having a fiber.

An optical information analysis apparatus according to an eleventh aspect of the present invention is the optical information analysis apparatus according to any one of the first to tenth aspects of the present invention described above, wherein the direction and position of the optical axis of the irradiation unit are adjusted. In addition, an irradiation position adjusting mechanism for adjusting a distance between the irradiation unit and the light receiving surface of the transmitted light receiving unit so as to satisfy the relational expression is further provided.

の関係式を満たすように調整する工程と、を備えていることを特徴とする。 In the optical information analysis method according to the first aspect of the present invention, a liquid in which a sample to be measured is dispersed is introduced into a flow cell of a flow cell by an introduction nozzle, and is dispersed in the liquid flowing in the flow path. An optical information analysis method for measuring optical information of the specimen by irradiating the specimen with single mode irradiation light, (a) provided at a position facing the irradiation section via the flow cell. In addition, the optical axis of the optical fiber of the transmitted light receiving unit that receives the transmitted light of the liquid by the irradiated light irradiated from the irradiation unit and detects it as a transmitted light signal substantially coincides with the optical axis of the irradiated unit. And (b) the core diameter of the optical fiber is d, the cladding diameter of the optical fiber is d ′, and the irradiation diameter of the irradiation light irradiated from the irradiation section on the light receiving surface of the optical fiber is is D, the light When the D'irradiation outer diameter of the irradiated the illumination light from the irradiation unit in the light-receiving surface of Aiba,

And a step of adjusting so as to satisfy the relational expression.

The optical information analysis method according to the second aspect of the present invention is the optical information analysis method according to the first aspect of the present invention described above. (C) After the step (b), the irradiation unit and the transmitted light A step of relatively adjusting the position of the sample flow by the liquid in the flow channel with respect to the measurement region in the flow channel determined based on the configuration of the light receiving unit is provided.

The optical information analysis method according to the third aspect of the present invention is the optical information analysis method according to the second aspect of the present invention described above, wherein the step (c) is such that the approximate center of the sample flow is the measurement region. The position of the sample flow in the channel is relatively adjusted so as to pass through the approximate center of the channel.

The optical information analysis method according to the fourth aspect of the present invention is the optical information analysis method according to the second aspect of the present invention described above, wherein (d) before the step (c), irradiation is performed from the irradiation unit. One or more scattering / fluorescence light receiving sections provided at positions not facing the irradiation section that detect side scattered light and / or fluorescence of the specimen by the irradiation light and detect it as a scattering / fluorescence signal. A step of causing the approximate center of the second measurement region determined based on the configuration to coincide with the approximate center of the measurement region, wherein in the step (c), the approximate center of the sample flow passes through the approximate center of the measurement region. As described above, the position of the sample flow in the flow path is relatively adjusted.

The optical information analysis method according to the fifth aspect of the present invention is the optical information analysis method according to the second aspect of the present invention described above. (D) Before the step (c), the optical information analysis method is irradiated from the irradiation unit. One or more scattering / fluorescence light receiving sections provided at positions not facing the irradiation section that detect side scattered light and / or fluorescence of the specimen by the irradiation light and detect it as a scattering / fluorescence signal. A step of causing the approximate center of the second measurement region determined based on the configuration to coincide with the approximate center of the measurement region, wherein the step (c) is configured such that the approximate center of the sample flow is greater than the approximate center of the measurement region. The position of the sample flow in the flow path is relatively adjusted so that it crosses the optical axis of the desired at least one scattering / fluorescence light receiving section and passes through a position away from the crossed scattering / fluorescence light receiving section. It is characterized by doing.

The optical information analysis method according to the sixth aspect of the present invention is the optical information analysis method according to the fourth or fifth aspect of the present invention, wherein the step (d) includes an optical axis of the scattering / fluorescence light receiving unit. And the optical axis of the irradiating part are substantially orthogonal within the measurement region.

An optical information analysis method according to a seventh aspect of the present invention is the optical information analysis method according to any one of the second to sixth aspects of the present invention described above, wherein the step (c) includes the flow of the flow cell. The position of the sample flow is adjusted with respect to the measurement region by a nozzle position adjusting mechanism that adjusts the position of the tip of the introduction nozzle in the passage.

An optical information analysis method according to an eighth aspect of the present invention is the optical information analysis method according to any one of the second to sixth aspects of the present invention, wherein the step (c) includes mounting the introduction nozzle. The position of the tip of the introduction nozzle in the flow channel of the flow cell is adjusted by being fixed to the flow cell. The position of the tip of the introduction nozzle in the flow path is adjusted so that the position of the desired sample flow with respect to the measurement region is obtained by the optimal offset jig selected from .

According to the optical information analysis device and the optical information analysis method of the present invention, by providing a transmitted light receiving unit that receives transmitted light at a position facing the irradiation unit, the sensitivity of the transmitted light received by the transmitted light receiving unit is increased. be able to.
Also, by aligning the optical axis of the transmitted light receiving unit with the optical axis of the irradiating unit and relatively adjusting the position of the sample flow so as to be orthogonal to the optical axis of the transmitted light receiving unit and the optical axis of the irradiating unit Thus, the sensitivity of the transmitted light received by the transmitted light receiving unit can be increased, and the optical information of the sample with little variation can be obtained.

In addition, the position of the sample flow is relatively adjusted so that it is perpendicular to the crossing position of the optical axis of the scattering / fluorescence light receiving part and the optical axis of the irradiation part that receives side scattered light and fluorescence. The sensitivity of the side scattered light and fluorescence received by the unit can be increased, and the optical information of the sample with little variation can be obtained.
Depending on the specimen, the light receiving efficiency of the fluorescent component of the surface antibody can also be improved.

It is a schematic longitudinal cross-sectional view of the optical information analysis apparatus which concerns on one Embodiment of this invention. FIG. 2 is a schematic longitudinal sectional view of the optical information analysis apparatus of FIG. 1 rotated 90 degrees around the Z axis. It is a schematic cross-sectional view in the KK line | wire of the optical information analyzer of FIG.1 and FIG.2. It is a figure for demonstrating position adjustment in the case of analyzing the sample S which should improve the light reception efficiency of the fluorescence component of a surface antibody. FIG. 4 is a flowchart for explaining an optical information analysis processing procedure for a specimen S using the optical information analysis apparatus 10 according to the embodiment of the present invention shown in FIGS. 1 to 3. It is a schematic longitudinal cross-sectional view of another optical information analyzer which concerns on one Embodiment of this invention. FIG. 7 is a schematic longitudinal sectional view of the optical information analysis apparatus of FIG. 6 rotated 90 degrees around the Z axis. It is a schematic cross-sectional view in the KK line of the optical information analysis apparatus of FIG.6 and FIG.7. It is a figure for demonstrating an offset jig | tool. It is another figure for demonstrating an offset jig | tool. It is a figure for demonstrating the optimal offset jig | tool when analyzing the sample S which should improve the light reception efficiency of the fluorescence component of a surface antibody. FIG. 9 is a flowchart for explaining an optical information analysis processing procedure for a specimen S using another optical information analysis apparatus 10a according to an embodiment of the present invention shown in FIGS. 6 to 8;

Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings.
FIG. 1 is a schematic longitudinal sectional view of an optical information analysis apparatus according to an embodiment of the present invention. 2 is a schematic longitudinal sectional view of the optical information analysis apparatus of FIG. 1 rotated 90 degrees around the Z axis. FIG. 3 is a KK line of the optical information analysis apparatus of FIGS. FIG.

  As shown in FIGS. 1 to 3, an optical information analysis apparatus 10 according to an embodiment of the present invention includes a flow cell 12 having a flow path 13a and a flow path 14a through which a liquid A flows, and a specimen storage unit (not shown). Single-mode irradiation light (excitation light) L0 to the introduction nozzle 15 for introducing the liquid A into the flow path 13a of the flow cell 12 and the sample S to be measured dispersed in the liquid A flowing through the flow path 14a of the flow cell 12. Irradiation unit 30 for irradiating, transmitted light receiving unit 50 for receiving the transmitted light L1 transmitted through the sample S by the excitation light and detecting it as a transmitted light signal SG1, and receiving the side scattered light and the fluorescence L2 from the sample S The scattered / fluorescent light receiving unit 60 detected as the scattered / fluorescent signal SG2, the irradiation position adjusting mechanism 70 for adjusting the position of the irradiating unit 30, and the position of the tip 15a of the introduction nozzle 15 are transmitted to the transmitted light receiving unit 50 and the illumination light. Based on the nozzle position adjusting mechanism 80 that adjusts to the unit 30, the transmitted light signal SG1 detected by the transmitted light receiving unit 50, and the scattered / fluorescent signal SG2 detected by the scattered / fluorescent light receiving unit 60, The irradiation unit 30 irradiates the sample S dispersed in the liquid A flowing in the flow path with non-collected irradiation light L0, which includes an analysis unit 90 that measures optical information and analyzes the sample S. Thus, the optical information of the specimen S is measured based on the transmitted light signal SG1 and the scattered / fluorescent signal SG2 of the specimen S detected by the transmitted light receiving section 50 and the scattering / fluorescence receiving section 60.

  In this specification, the transmitted light is received by the transmitted light receiving unit such as light that has passed through the liquid in which the specimen is dispersed, light that has passed through the specimen, and light that has been reflected, scattered, and diffracted by the specimen. Light is called transmitted light. The transmitted light signal is a signal obtained by converting transmitted light into an electrical signal, and the scattered / fluorescent signal is a signal obtained by converting side scattered light and / or fluorescence into an electrical signal. Further, in an arbitrary region that receives transmitted light, light is received, and the amount of received light (transmitted light signal) varies during sample measurement. The peak, width, area, etc. of the fluctuation are called optical information. In addition, the peak, width, area, and the like of fluctuations in the amount of side scattered light and / or fluorescence received (scattered / fluorescent signal) during sample measurement are also referred to as optical information.

  The flow cell 12 creates a flow 11B of the sheath liquid B so as to surround the flow of the liquid A in which the specimen S is dispersed, and forms a flow 11A of the liquid A that is linear in the Z direction. And a capillary part 14 having a flow path 14a that is linear in the Z direction and has a rectangular cross section perpendicular to the Z direction, which maintains the flow 11A of the liquid A that is linear in the Z direction. The tapered portion 13 and the capillary portion 14 are integrated so that the flow channel 13a and the flow channel 14a are continuous. The flow cell 12 is made of glass or transparent resin.

  In the present specification, the sample flow refers to the flow 11A of the sample liquid A when the liquid (sample liquid) A containing the specimen S flows through the flow path 13a and the flow path 14a of the flow cell 12, and the sheath The flow is a flow 11B of the sheath liquid B surrounding the sample flow. The direction of the sample flow 11A is the Z direction. In addition, the optical axis direction (direction of the optical axis 51a of the optical fiber 51) and the optical axis direction of the irradiation unit 30 (direction of the optical axis 31a of the optical fiber 31) are orthogonal to the Z direction and are described later. ) Is the direction substantially parallel to the X direction. A direction orthogonal to the Z direction and the X direction is defined as a Y direction.

  The introduction nozzle 15 introduces the sample liquid A from the specimen storage unit (not shown) into the flow path 13a of the flow cell 12. Further, the introduction nozzle 15 is moved by the nozzle position adjusting mechanism 80 so that the distal end portion 15a is moved in the flow path 13a of the flow cell 12 in the X direction (arrow 20a direction), Y direction (arrow 20b direction), and Z direction (arrow 20c direction). ) To freely adjust the position of the tip portion 15a.

  The irradiation unit 30 propagates the irradiation light L0 through the semiconductor laser element 32 that emits laser light having a predetermined wavelength (for example, light of 488 nm) as irradiation light (excitation light) L0 and flows in the flow path 14a. And an optical fiber 31 that emits in the vicinity of the flow (sample flow) 11A of the sample liquid A. The optical fiber 31 is configured such that the optical axis 31a is substantially in the X direction orthogonal to the Z direction. In addition, although the irradiation part 30 is the structure which has the optical fiber 31, what is necessary is just an irradiation part of the structure whose optical axis is a substantially X direction substantially orthogonal to a Z direction.

  The transmitted light receiver 50 receives the transmitted light L1 from the specimen S in the vicinity of the sample stream 11A, the transmitted light L1 propagated through the optical fiber 51, and detects it as a transmitted light signal SG1, And a light receiving element 52 that transmits the detected transmitted light signal SG1 to the analyzing unit 90. Examples of the light receiving element 52 include a photomultiplier tube and a photodetector.

  The optical fiber 51 is provided at a position facing the optical fiber 31 via the capillary portion 14 of the flow cell 12. Here, the directly facing position means that the light receiving surface 51b of the optical fiber 51 orthogonal to the optical axis 51a and the end surface 31b of the optical fiber 31 orthogonal to the optical axis 31a are provided so as to face each other, and irradiation is performed. The optical axis 31a of the optical fiber 31 of the part 30 and the optical axis 51a of the optical fiber 51 of the transmitted light receiving part 50 are substantially parallel.

  The optical axis 31a of the optical fiber 31 of the irradiation unit 30 described above is moved in the Y direction (arrow 21b direction) and the Z direction (arrow 21c direction) by the irradiation position adjusting mechanism 70. Thus, it is desirable that the optical axis 51a of the optical fiber 51 of the transmitted light receiving unit 50 is substantially aligned. The optical fiber 51 is fixed to the flow cell 12.

  Further, the optical fiber 51 has an optical axis 51a that is substantially in the X direction substantially orthogonal to the Z direction and passes through the approximate center O of the flow path 14a of the capillary portion 14 on a plane substantially orthogonal to the Z direction. Is provided.

  The transmitted light receiving unit 50 includes the optical fiber 51. However, the optical axis of the transmitted light receiving unit is substantially the X direction substantially orthogonal to the Z direction, and the transmitted light receiving unit approximately orthogonal to the optical axis. It is sufficient that the light receiving surface of the light receiving unit is configured to face the irradiation unit 30 and the center of the light receiving surface of the transmitted light receiving unit substantially coincides with the optical axis of the irradiation unit 30.

  At this time, the diameter d ″ of the light receiving surface of the transmitted light receiving unit 50 and the irradiation diameter D of the irradiation light L0 irradiated from the irradiation unit 30 on the light receiving surface b of the transmitted light receiving unit 50 are expressed by the following relational expression: (1) is satisfied.

上記の関係式（１）によって、透過光Ｌ１を透過光受光部５０が受光することで照射部３０の光軸３１ａとの最適位置関係や透過光信号変動が高感度に受光できるようになり、透過光受光部５０で検出した透過光信号ＳＧ１の感度を増加させることができる。ここで、照射径Ｄは、ビーム径のことで、ビーム中心強度の１／ｅ²（＝１３．５％）強度の直径をいう。

According to the above relational expression (1), when the transmitted light receiving unit 50 receives the transmitted light L1, the optimum positional relationship with the optical axis 31a of the irradiation unit 30 and the transmitted light signal fluctuation can be received with high sensitivity. The sensitivity of the transmitted light signal SG1 detected by the transmitted light receiving unit 50 can be increased. Here, the irradiation diameter D is a beam diameter, which is a diameter having an intensity of 1 / e ² (= 13.5%) of the beam center intensity.

  As shown in FIGS. 1, 2, and 3, when the transmitted light receiving unit 50 has an optical fiber 51, the core diameter d of the core 51 c of the optical fiber 51 and the light receiving surface 51 b of the optical fiber 51 are used. It is desirable that the irradiation diameter D of the irradiation light L0 irradiated from the irradiation unit 30 is configured so that the following relational expression (2) is satisfied.

上記の関係式（２）によって、透過光Ｌ１を透過光受光部５０の光ファイバ５１が受光することで照射部３０の光軸３１ａとの最適位置関係や透過光信号変動が高感度に受光できるようになり、受光素子５２で検出した透過光信号ＳＧ１の感度を増加させることができる。ここで、コア径ｄは、ＪＩＳ Ｃ ６８２０（光ファイバ通則）に準ずる。

According to the above relational expression (2), when the optical fiber 51 of the transmitted light receiving unit 50 receives the transmitted light L1, the optimum positional relationship with the optical axis 31a of the irradiation unit 30 and the transmitted light signal fluctuation can be received with high sensitivity. Thus, the sensitivity of the transmitted light signal SG1 detected by the light receiving element 52 can be increased. Here, the core diameter d conforms to JIS C 6820 (general rules for optical fibers).

  Further, the following relational expression (3) is established between the cladding diameter d ′ of the cladding 51 d of the optical fiber 51 and the irradiation outer diameter D ′ of the irradiation light L 0 irradiated from the irradiation unit 30 on the light receiving surface 51 b of the optical fiber 51. Further, it is desirable to be configured to hold.

上記の関係式（３）によって、透過光Ｌ１を透過光受光部５０の光ファイバ５１が受光することで照射部３０の光軸３１ａとの最適位置関係や透過光信号変動が、更に高感度に受光できるようになり、受光素子５２で検出した透過光信号ＳＧ１の感度を更に増加させることができる。また、照射光Ｌ０の迷光を防ぐことができる。ここで、クラッド径ｄ´は、ＪＩＳ Ｃ ６８２０（光ファイバ通則）に準ずる。また、照射外郭径Ｄ´は、ビーム中心強度の５％強度の直径をいう。

According to the above relational expression (3), when the optical fiber 51 of the transmitted light receiving unit 50 receives the transmitted light L1, the optimum positional relationship with the optical axis 31a of the irradiating unit 30 and the transmitted light signal fluctuation are further enhanced. Light can be received, and the sensitivity of the transmitted light signal SG1 detected by the light receiving element 52 can be further increased. Further, stray light from the irradiation light L0 can be prevented. Here, the cladding diameter d ′ conforms to JIS C 6820 (General rules for optical fibers). Further, the irradiation outer diameter D ′ refers to a diameter that is 5% of the beam center intensity.

  It should be noted that the irradiation position adjusting mechanism 70 causes the irradiation unit 30 to satisfy the relational expression (1), the relational expression (2), and the relational expression (3). You may make it adjust by moving the position of the optical fiber 31 to a X direction (arrow 21a direction).

  The scattering / fluorescence light receiving unit 60 receives the side scattered light and / or fluorescence L2 from the specimen in the vicinity of the sample flow 11A, and the side scattered light and / or fluorescence L2 propagated through the optical fiber 61. A light receiving element 62 that receives light, detects it as a scattered / fluorescent signal SG2, and transmits the detected scattered / fluorescent signal SG2 to the analyzing unit 90 is provided. Examples of the light receiving element 62 include a photomultiplier tube and a photodetector. It is desirable that a plurality of light receiving elements 62 be provided, and the side scattered light and / or fluorescence separated for each wavelength by an optical filter or the like be received by the plurality of light receiving elements 62. At this time, each light receiving element 62 detects a different scattered / fluorescent signal SG 2, and a plurality of scattered / fluorescent signals SG 2 detected by each light receiving element 62 are sent to the analysis unit 90. 1 to 3, the optical information analysis apparatus 10 includes only one scattering / fluorescence light receiving unit 60, but a plurality of similar scattering / fluorescence light receiving units may be provided.

The optical fiber 61 is such that the optical axis 61a is substantially orthogonal to the optical axis 51a of the optical fiber 51 and the optical axis 31a of the optical fiber 31 (that is, substantially orthogonal to the X direction) and substantially orthogonal to the Z direction. It is provided so as to pass through the approximate center O of the flow path 14a of the capillary portion 14 on a plane that is approximately in the Y direction and orthogonal to the Z direction. The optical fiber 61 is fixed to the flow cell 12. The scattering / fluorescence light receiving unit 60 does not necessarily need to be orthogonal to the optical axis 51a or the optical axis 31a, and may be provided so as to intersect.
Further, the optical fibers 51 and 61 may be arranged so that the light receiving surfaces 51b and 61b are in direct contact with the sheath flow 11B.

  The nozzle position adjusting mechanism 80 is configured such that the center of the sample flow 11A is the position where the optical axis 51a of the optical fiber 51, the optical axis 31a of the optical fiber 31, and the optical axis 61a of the optical fiber 61 intersect (capillary on a plane perpendicular to the Z direction). In the flow channel 13a of the flow cell 12, the tip portion 15a of the introduction nozzle 15 is moved in the X direction (arrow 20a direction), the Y direction (arrow 20b direction), and the flow path 12a. The position of the tip 15a of the introduction nozzle 15 is adjusted by moving in the Z direction (direction of the arrow 20c). That is, by adjusting the position of the distal end portion 15a of the introduction nozzle 15 by the nozzle position adjusting mechanism 80, the position where the optical axis 51a of the optical fiber 51, the optical axis 31a of the optical fiber 31, and the optical axis 61a of the optical fiber 61 intersect ( The position of the sample flow 11A in the flow path 14a is adjusted to the optimum position with respect to the measurement region that is the region of the transmitted light L1 (irradiation light L0) in the vicinity of the approximate center O).

  In the present specification, the center of the sample flow 11A is a center position within the passage range of the sample flow 11A on a plane orthogonal to the flow direction (Z direction) of the sample flow 11A. Further, the position of the sample flow 11A in the flow channel 14a refers to the surface in the flow channel 14a that passes through the center O of the measurement region in the flow channel 14a and is orthogonal to the flow direction (Z direction) of the sample flow 11A. Is the position through which the center of the sample flow 11A passes. The measurement region is determined based on the diameter of the irradiation light irradiated from the irradiation unit in the flow path, the light receiving region of the transmitted light receiving unit, and the scattering / fluorescence receiving unit.

  Further, the optimum position is that the transmitted light signal SG1 and the scattered / fluorescent signal SG2 of the specimen S detected in the transmitted light receiving section 50 and the scattering / fluorescence receiving section 60 can be detected with the highest sensitivity. This is the position where the optical information of the specimen S measured based on the transmitted light signal SG1 and the scattered / fluorescent signal SG2 has the least variation. Therefore, the position of the sample flow 11A in the flow channel 14a is adjusted to an optimum position while actually irradiating the sample flow 11A in the flow channel 14a with irradiation light (excitation light). That is, adjustment is made so that the center of the sample flow 11A is aligned with the position (substantially center O) where the optical axis 51a of the optical fiber 51, the optical axis 31a of the optical fiber 31, and the optical axis 61a of the optical fiber 61 intersect.

  The optimum position of the sample flow 11A described above is the case where the optical axis 51a of the optical fiber 51, the optical axis 31a of the optical fiber 31, and the optical axis 61a of the optical fiber 61 intersect (substantially the center O). However, depending on the specimen S, in order to improve the light receiving efficiency of the fluorescent component of the surface antibody, as shown in FIG. 4, the optical axis 51a of the optical fiber 51, the optical axis 31a of the optical fiber 31, and the optical axis of the optical fiber 61 In some cases, the position O ′ is further away from the light receiving surface 61b of the optical fiber 61 in the Y direction than the position where the 61a intersects (substantially the center O). In such a case, adjustment may be made so that the position O ′ and the center of the sample flow 11A are aligned.

  The analyzing unit 90 measures the light information of the specimen S based on the transmitted light signal SG1 detected by the transmitted light receiving unit 50 and the scattered / fluorescent signal SG2 detected by the scattered / fluorescent light receiving unit 60, and the measured light The specimen S is analyzed based on the information. Further, the analysis unit 90 may transmit the analysis result of the sample S to a dispensing unit (not shown) that dispenses the sample S based on the analysis result.

  The optical information analysis apparatus 10 according to an embodiment of the present invention shown in FIGS. 1 to 3 has a configuration including the scattering / fluorescence light receiving unit 60, but may be configured without the scattering / fluorescence light receiving unit 60. good.

  The sensitivity of the transmitted light signal SG1 detected by the transmitted light receiving unit 50 can be increased by the optical information analyzing apparatus 10 according to the embodiment of the present invention described above. Further, the sensitivity of the scattering / fluorescence signal SG2 detected by the scattering / fluorescence light receiving unit 60 can be increased. Further, the analyzing unit 90 can measure the optical information of the sample S with little variation based on the transmitted light signal SG1 and the scattered / fluorescent signal SG2 detected by the transmitted light receiving unit 50 and the scattered / fluorescent light receiving unit 60. it can. In addition, depending on the specimen S, the light receiving efficiency of the fluorescent component of the surface antibody can be improved.

Next, a procedure for optical information analysis processing of the specimen S using the optical information analysis apparatus 10 according to the embodiment of the present invention shown in FIGS. 1 to 3 will be briefly described.
FIG. 5 is a flowchart for explaining the optical information analysis processing procedure of the specimen S using the optical information analysis apparatus 10 according to the embodiment of the present invention shown in FIGS. 1 to 3.

  As shown in FIG. 5, first, irradiation light L0 is irradiated from the irradiation unit 30 to the capillary unit 14 of the flow cell 12 (step 1: S101), and the position of the optical fiber 31 of the irradiation unit 30 is adjusted by the irradiation position adjusting mechanism 70. Are moved in the Y direction and the Z direction so that the optical axis 51a of the optical fiber 51 of the transmitted light receiving unit 50 fixed to the flow cell 12 and the optical axis 31a of the optical fiber 31 of the irradiation unit 30 substantially coincide with each other. Adjust (step 2: S102). Further, the position of the optical fiber 31 of the irradiation unit 30 is adjusted by the irradiation position adjusting mechanism 70 so that the optical axis 31a of the optical fiber 31 and the optical axis 61a of the optical fiber 61 intersect each other at a substantially center O (see FIG. 4). You may do it. That is, the approximate center of the second measurement region of the scattering / fluorescence light receiving unit 60 and the approximate center of the measurement region of the transmitted light receiving unit 50 may be adjusted to coincide.

  The optical axis 51a of the optical fiber 51 of the transmitted light receiving unit 50 passes through the approximate center O of the flow path 14a of the capillary unit 14, is parallel to the X direction, and is arranged with high accuracy so as to be orthogonal to the Z direction. (See FIGS. 1 and 3). The position where the optical axis 51 a of the optical fiber 51 of the transmitted light receiving unit 50 substantially coincides with the optical axis 31 a of the optical fiber 31 of the irradiating unit 30 means that the transmitted light receiving unit 50 receives light irradiated from the irradiating unit 30. The position where the amount is maximum. Further, the adjustment of the position of the optical fiber 31 of the irradiation unit 30 is desirably performed in a state where the sheath liquid B or the sample liquid A is allowed to flow in the flow path 14 a of the capillary unit 14.

  Next, the position of the optical fiber 31 of the irradiation unit 30 is moved in the X direction by the irradiation position adjusting mechanism 70, and adjustment is performed so that the above relational expression (1) is established (step 3: S103). Here, in the irradiation unit 30, when irradiation is performed using a lens without using the optical fiber 31, the center of the irradiation region determined by the constituent lens is made to substantially coincide with the center O of the flow path 14 a of the capillary unit 14. The adjustment is made so that the above relational expression (1) is established. In Step 3, it is desirable to adjust so that the above relational expression (2) is established. Further, in step 3, it is desirable to further adjust so that the above relational expression (3) is satisfied.

  Next, the sample liquid A adjusted so that the relative position of the sample S with respect to the irradiation light L0 from the irradiation unit 30 changes at a constant speed is used as the sample flow 11A, and the flow of the flow cell 12 from the sample storage unit (not shown). It introduce | transduces into the path | route 13a through the introduction nozzle 15 (step 4: S104). Note that the processing timing of step 4 for introducing the sample liquid A into the flow path 13a of the flow cell 12 via the introduction nozzle 15 is not limited to the timing of this flowchart, and may be, for example, before step 1 described above. Any timing may be used as long as it is before step 5 described later.

  Next, the nozzle position adjusting mechanism 80 causes the center of the sample flow 11A to pass through the position (center O) where the optical axis 51a of the optical fiber 51, the optical axis 31a of the optical fiber 31, and the optical axis 61a of the optical fiber 61 intersect. In addition, the tip 15a of the introduction nozzle 15 is moved in the X direction, the Y direction, and the Z direction in the flow path 13a of the flow cell 12 to adjust the position of the tip 15a of the introduction nozzle 15 (step 5: S105). ).

  The optical axis 61a of the optical fiber 61 of the scattering / fluorescence light receiving unit 60 passes through the approximate center O of the flow path 14a of the capillary unit 14, is parallel to the Y direction, and is orthogonal to the Z direction with high accuracy. (See FIGS. 2 and 3). When the scattering / fluorescence light receiving unit 60 receives light using a lens without using the optical fiber 61, the center of the scattering / fluorescence light receiving region determined by the constituent lenses is the center O of the flow path 14 a of the capillary unit 14. It arrange | positions so that it may correspond substantially.

  In addition, as shown in FIG. 4, when analyzing the specimen S in which the light receiving efficiency of the fluorescent component of the surface antibody is better, the center of the sample flow 11A is the optical axis 51a of the optical fiber 51, the optical fiber The tip of the introduction nozzle 15 passes through a position O ′ that is further away from the light receiving surface 61b of the optical fiber 61 in the Y direction than the position (substantially the center O) where the optical axis 31a of the optical fiber 31 and the optical axis 61a of the optical fiber 61 intersect. 15 a is moved in the X direction, the Y direction, and the Z direction in the flow path 13 a of the flow cell 12 to adjust the position of the tip portion 15 a of the introduction nozzle 15.

  Next, the transmitted light receiving unit 50 receives the transmitted light L1, detects it as a transmitted light signal SG1, and transmits the detected transmitted light signal SG1 to the analyzing unit 90, while the scattered / fluorescent light receiving unit 60 causes the side. The scattered light and / or fluorescence L2 is received and detected as the scattered / fluorescent signal SG2, and the detected scattered / fluorescent signal SG2 is transmitted to the analyzing unit 90 (step 6: S106).

  Finally, the analyzing unit 90 measures the light information of the sample S based on the transmitted light signal SG1 and the scattered / fluorescent signal SG2, and analyzes the sample S based on the measured light information (step 7: S107). The optical information analysis processing procedure for the specimen S using the optical information analysis apparatus 10 according to the embodiment of the present invention shown in FIGS. 1 to 3 is finished. In addition, after step 7, processing for dispensing the sample S may be performed based on the result analyzed in step 7. Further, it is not necessary to perform Step 1 to Step 5 every time at the time of analysis (to perform Step 6 and Step 7).

  The sensitivity of the transmitted light signal SG1 detected by the transmitted light receiving unit 50 can be increased by the optical information analysis processing procedure of the sample S in FIG. Further, the sensitivity of the scattering / fluorescence signal SG2 detected by the scattering / fluorescence light receiving unit 60 can be increased. Further, the analyzing unit 90 can measure the optical information of the sample S with little variation based on the transmitted light signal SG1 and the scattered / fluorescent signal SG2 detected by the transmitted light receiving unit 50 and the scattered / fluorescent light receiving unit 60. it can. In addition, depending on the specimen S, the light receiving efficiency of the fluorescent component of the surface antibody can be improved.

Next, another optical information analysis apparatus 10 according to an embodiment of the present invention will be described with reference to FIGS.
FIG. 6 is a schematic longitudinal sectional view of another optical information analysis apparatus according to an embodiment of the present invention. 7 is a schematic longitudinal sectional view of the optical information analysis apparatus of FIG. 6 rotated 90 degrees around the Z axis, and FIG. 8 is a KK line of the optical information analysis apparatus of FIGS. FIG. 9 to 11 are views for explaining the offset jig.

The difference between another optical information analysis apparatus 10a according to one embodiment of the present invention shown in FIGS. 6 to 8 and the optical information analysis apparatus 10 according to one embodiment of the present invention shown in FIGS. Instead of the nozzle position adjusting mechanism 80 that adjusts the position of the tip 15a of the introduction nozzle 15 according to the transmitted light receiving unit 50 and the irradiation unit 30, the position of the tip 15a of the introduction nozzle 15 is changed to the transmitted light receiving unit 50 and A plurality of offset jigs 100 _i (i = 1 to n) to be adjusted in accordance with the irradiation unit 30 are provided, and an optimum offset jig 100 _a is selected from the offset jigs 100 _i (i = 1 to n). The introduction nozzle 15 is mounted on the selected offset jig 100 _a and fixed to the upper end portion 13 b of the tapered portion 13 of the flow cell 12.

For example, as shown in FIGS. 9A to 9C and FIGS. 10A to 10C, the offset jig 100 _i (i = 1 to n) is provided with an introduction nozzle 15 and a flow cell. By fixing to the upper end part 13b of the 12 taper parts 13, the position of the front-end | tip part 15a of the introduction nozzle 15 is adjusted. That is, as shown in FIG. 8, when the introduction nozzle 15 is mounted and fixed to the upper end portion 13b of the tapered portion 13 of the flow cell 12, the center of the sample flow 11A is the optical axis 51a of the optical fiber 51 and the optical fiber 31. An optimum offset jig 100 _a passing through a position (center O) where the optical axis 31 a and the optical axis 61 a of the optical fiber 61 intersect is selected from a plurality of offset jigs 100 _i (i = 1 to n) and selected. use the optimum offset jig 100 _a, to measure the optical information of the specimen S.

Further, when analyzing the sample S for which it is better to improve the light receiving efficiency of the fluorescent component of the surface antibody, as shown in FIG. 11, the introduction nozzle 15 is attached and the upper end portion 13 b of the tapered portion 13 of the flow cell 12 is attached. When fixed, the center of the sample flow 11A is more light-receiving surface 61b of the optical fiber 61 than the position (center O) where the optical axis 51a of the optical fiber 51, the optical axis 31a of the optical fiber 31, and the optical axis 61a of the optical fiber 61 intersect. The optimum offset jig 100 _b passing through the position O ′ away from the Y direction is selected from a plurality of offset jigs 100 _i (i = 1 to n), and the selected optimum offset jig 100 _b is selected. Used to measure the optical information of the specimen S.

The optimum offset jig 100 _a or offset jig 100 _b is selected by attaching the introduction nozzle 15 to various offset jigs 100 _i (i = 1 to n), and then the upper end of the tapered portion 13 of the flow cell 12. It is determined by the position of the actual sample flow 11A when fixed to the portion 13b.

  The sensitivity of the transmitted light signal SG1 detected by the transmitted light receiving unit 50 can be increased by the other optical information analyzing apparatus 10a according to the embodiment of the present invention described above. Further, the sensitivity of the scattering / fluorescence signal SG2 detected by the scattering / fluorescence light receiving unit 60 can be increased. Further, the analyzing unit 90 can measure the optical information of the sample S with little variation based on the transmitted light signal SG1 and the scattered / fluorescent signal SG2 detected by the transmitted light receiving unit 50 and the scattered / fluorescent light receiving unit 60. it can. In addition, depending on the specimen S, the light receiving efficiency of the fluorescent component of the surface antibody can be improved.

Next, an optical information analysis processing procedure for the specimen S using another optical information analysis apparatus 10a according to an embodiment of the present invention shown in FIGS. 6 to 8 will be briefly described.
FIG. 12 is a flowchart for explaining the optical information analysis processing procedure of the specimen S using another optical information analysis apparatus 10a according to the embodiment of the present invention shown in FIG. 6 to FIG.

The optical information analysis processing procedure for the specimen S using another optical information analysis apparatus 10a according to the embodiment of the present invention shown in FIGS. 6 to 8 shown in FIG. 12, and FIGS. 1 to 3 shown in FIG. The difference from the optical information analysis processing procedure of the specimen S using the optical information analysis apparatus 10 according to the embodiment of the present invention shown in FIG. 5 is that in step 5, the nozzle position adjustment mechanism 80 causes the tip portion 15a of the introduction nozzle 15 to move. Instead of adjusting the position, when the introduction nozzle 15 is mounted and fixed to the upper end portion 13b of the tapered portion 13 of the flow cell 12, the center of the sample flow 11A is the optical axis 51a of the optical fiber 51 and the light of the optical fiber 31. optical axis 61a intersects the axis position 31a and the optical fiber 61 an optimum offset jig 100 _a through a (substantially the center O), selected from a plurality of offset jigs 100 _{i (i} = 1~n), selected And the injection nozzle 15 in offset jig 100 _a fitted, is to fix the upper end portion 13b of the tapered portion 13 of the flow cell 12.

Further, when analyzing the sample S for which it is better to improve the light receiving efficiency of the fluorescent component of the surface antibody, as shown in FIG. 11, the introduction nozzle 15 is attached and the upper end portion 13 b of the tapered portion 13 of the flow cell 12 is attached. When fixed, the center of the sample flow 11A is more light-receiving surface of the optical fiber 61 than the position where the optical axis 51a of the optical fiber 51, the optical axis 31a of the optical fiber 31 and the optical axis 61a of the optical fiber 61 intersect (substantially center O). The optimum offset jig 100 _b passing through the position O ′ away from 61b in the Y direction is selected from a plurality of offset jigs 100 _i (i = 1 to n), and the selected optimum offset jig 100 _{b is selected.} Is used to measure the optical information of the specimen S.

The optimum offset jig 100 _a or offset jig 100 _b is selected by attaching the introduction nozzle 15 to various offset jigs 100 _i (i = 1 to n), and then the upper end of the tapered portion 13 of the flow cell 12. It is determined by the position of the actual sample flow 11A when fixed to the portion 13b.

  Note that the processing timing of step 4 for introducing the sample liquid A into the flow path 13a of the flow cell 12 via the introduction nozzle 15 is not limited to the timing of this flowchart, and may be, for example, before step 1 described above. As long as it is before step 5, any timing may be used. Further, the adjustment of the position of the optical fiber 31 of the irradiation unit 30 in Step 2 is desirably performed in a state where the sheath liquid B or the sample liquid A is allowed to flow in the flow path 14 a of the capillary section 14. Further, it is not necessary to perform Step 1 to Step 5 every time at the time of analysis (to perform Step 6 and Step 7).

  The sensitivity of the transmitted light signal SG1 detected by the transmitted light receiving unit 50 can be increased by the optical information analysis processing procedure of the sample S in FIG. 12 described above. Further, the sensitivity of the scattering / fluorescence signal SG2 detected by the scattering / fluorescence light receiving unit 60 can be increased. Further, the analyzing unit 90 can measure the optical information of the sample S with little variation based on the transmitted light signal SG1 and the scattered / fluorescent signal SG2 detected by the transmitted light receiving unit 50 and the scattered / fluorescent light receiving unit 60. it can. In addition, depending on the specimen S, the light receiving efficiency of the fluorescent component of the surface antibody can be improved.

The optical information analysis device 10 shown in FIGS. 1 to 3 and the optical information analysis device 10a shown in FIGS. 6 to 8 include a transmitted light receiving unit 50 and an irradiation unit using a nozzle position adjusting mechanism 80 and an offset jig 100 _i . Although the position of the tip 15a of the introduction nozzle 15 is directly moved according to 30, the position of the tip 15a of the introduction nozzle 15 is relatively moved according to the transmitted light receiving part 50 and the irradiation part 30. The flow cell 12, the transmitted light receiving unit 50 and the scattering / fluorescence receiving unit 60 fixed to the flow cell 12, and the irradiation unit 30 whose position is adjusted with respect to the transmitted light receiving unit 50 are combined together. It may be an optical information analysis device having a configuration including an adjustment unit that is moved with respect to the position of the distal end portion 15a.

  An optical information analysis apparatus and an optical information analysis method according to an embodiment of the present invention include fields that require examination, analysis, and analysis of biopolymers of genes, immune systems, proteins, amino acids, and sugars, such as engineering fields, foods, and the like. It can be applied to all fields such as agriculture, general agriculture such as fishery processing, pharmacy, sanitation, health, immunity, plague, genetics such as heredity, and science such as chemistry or biology.

DESCRIPTION OF SYMBOLS 10, 10a: Optical information analyzer 11A: Sample flow 11B: Sheath flow 12: Flow cell 13: Taper part 13a, 14a: Flow path 14: Capillary part 15: Introducing nozzle 30: Irradiation part 31, 51, 61: Optical fiber 50 : Transmitted light receiving unit 60: Scattering / fluorescence receiving unit 70: Irradiation position adjustment mechanism 80: Nozzle position adjustment mechanism 90: Analysis unit 100 _i (i = 1 to n): Offset jig S: Sample L0: Irradiation light L1: Transmitted light L2: Side scattered light and / or fluorescence SG1: Transmitted light signal SG2: Scattered / fluorescent signal

Claims (19)

An optical information analyzer for measuring optical information of the specimen by irradiating the specimen to be measured dispersed in the liquid flowing in the flow path with single mode irradiation light,
A flow cell having the flow path;
An introduction nozzle for introducing the liquid into the flow path of the flow cell;
An irradiation unit that irradiates the irradiation light to the liquid flowing through the flow path of the flow cell;
A transmitted light receiving unit provided at a position facing the irradiation unit via the flow cell, receiving the transmitted light of the liquid by the irradiation light irradiated from the irradiation unit and detecting it as a transmitted light signal;
Based on the transmitted light signal detected by the transmitted light receiving unit, the optical information of the specimen is measured and analyzed,
Have
The transmitted light receiving unit includes an optical fiber disposed so that a light receiving surface substantially orthogonal to an optical axis faces the irradiation unit, and a center of the light receiving surface substantially coincides with an optical axis of the irradiation unit,
The core diameter of the optical fiber is d, the cladding diameter of the optical fiber is d ′, the irradiation diameter of the irradiation light irradiated from the irradiation unit on the light receiving surface of the optical fiber is D , and the optical fiber When the irradiation outer diameter of the irradiation light irradiated from the irradiation unit on the light receiving surface is D ′,

An optical information analysis device characterized by satisfying the relational expression: An adjustment unit that adjusts the position of the sample flow caused by the liquid in the flow channel relative to a measurement region in the flow channel determined based on the configuration of the irradiation unit and the transmitted light receiving unit; it is an optical information analysis apparatus according to claim 1, wherein the. Receiving the side scattered light and / or fluorescence of the specimen by the irradiation light irradiated from the irradiation unit and detecting it as a scattering / fluorescence signal, the irradiation unit whose optical axis intersects the optical axis of the irradiation unit; the scattering and fluorescent light receiving portion provided at a position not confronting the optical information analyzing device according to claim 1 or 2, characterized in that it comprises one or more further. The optical information analysis apparatus according to claim 3 , wherein the scattering / fluorescence light receiving unit includes an optical fiber disposed such that a light receiving surface substantially orthogonal to an optical axis does not face the irradiation unit. . 5. The optical information analysis apparatus according to claim 3 , wherein an optical axis of the irradiation unit and an optical axis of the scattering / fluorescence light receiving unit are substantially orthogonal to each other. Approximate center of the sample flow, to pass through substantially the center of the measuring area, any one of claims 2 to 5, characterized in that relatively adjust the position of the sample flow in the channel The optical information analysis apparatus described in 1. The adjustment unit has an approximate center of the sample flow intersecting an optical axis of the desired at least one scattering / fluorescence light receiving unit, and separated from the intersecting scattering / fluorescence light receiving unit than the approximate center of the measurement region. The optical information analysis apparatus according to claim 3 , wherein the position of the sample flow in the flow path is relatively adjusted so as to pass through the position . The adjustment unit includes a nozzle position adjustment mechanism that adjusts the position of the tip of the introduction nozzle in the flow path of the flow cell;
3. The position of the sample flow is adjusted with respect to the measurement region by adjusting the position of the tip of the introduction nozzle in the flow path of the flow cell by the nozzle position adjusting mechanism. 8. The optical information analysis apparatus according to any one of items 1 to 7. The adjustment unit adjusts the position of the tip of the introduction nozzle in the flow path of the flow cell by mounting the introduction nozzle and fixing the introduction nozzle to the flow cell, and the position of the tip of the introduction nozzle is different Equipped with multiple offset jigs,
The position of the leading end portion of the introduction nozzle in the flow path so as to be a desired position of the sample flow with respect to the measurement region by the optimum offset jig selected from the plurality of offset jigs The optical information analysis device according to claim 2 , wherein the optical information analysis device is adjusted. The irradiation unit is optical information analyzing device according to any one of claims 1 to 9, characterized in that it comprises an optical fiber for propagating said radiation beam. While adjusting the direction and position of the optical axis of the irradiation unit, the so as to satisfy the relational expression, the irradiation position adjusting mechanism for adjusting the distance between the light receiving surface of the transmitted light receiving unit and the irradiation unit further comprises the optical information analyzing device according to any one of claims 1 to 10, characterized in that is. Introducing a liquid in which a specimen to be measured is dispersed into a flow cell of a flow cell by an introduction nozzle, and irradiating the specimen dispersed in the liquid flowing in the flow path with single-mode irradiation light An optical information analysis method for measuring optical information of the specimen,
(A) A transmitted light receiving unit provided at a position facing the irradiation unit via the flow cell and receiving the transmitted light of the liquid by the irradiation light irradiated from the irradiation unit and detecting it as a transmitted light signal Substantially matching the optical axis of the optical fiber with the optical axis of the irradiation section;
(B) The core diameter of the optical fiber is d, the cladding diameter of the optical fiber is d ′, the irradiation diameter of the irradiation light irradiated from the irradiation unit on the light receiving surface of the optical fiber is D, When the irradiation outer diameter of the irradiation light irradiated from the irradiation unit on the light receiving surface of the optical fiber is D ′,

Optical information analyzing method characterized in that comprises a, and adjusting to satisfy the relational expression. (C) After the step (b), the position of the sample flow by the liquid in the flow channel is determined with respect to the measurement region in the flow channel determined based on the configuration of the irradiation unit and the transmitted light receiving unit. The optical information analysis method according to claim 12 , further comprising a relative adjustment step . Wherein step (c), substantially the center of the sample flow, to pass through substantially the center of the measuring area, claim 13, characterized in that the adjusted relative position of the sample flow in the channel The optical information analysis method described in 1 . (D) Before the step (c), the irradiation unit that receives side scattered light and / or fluorescence of the specimen by the irradiation light irradiated from the irradiation unit and detects it as a scattered / fluorescent signal; A step of causing the approximate center of the second measurement region determined based on the configuration of one or more scattering / fluorescence light receiving units provided at positions not facing each other to coincide with the approximate center of the measurement region,
Wherein step (c), substantially the center of the sample flow, wherein to pass substantially the center of the measurement region, claim 13, characterized in that the relative adjustment of the position of the sample flow in the channel The optical information analysis method described in 1. (D) Before the step (c), the irradiation unit that receives side scattered light and / or fluorescence of the specimen by the irradiation light irradiated from the irradiation unit and detects it as a scattered / fluorescent signal; A step of causing the approximate center of the second measurement region determined based on the configuration of one or more scattering / fluorescence light receiving units provided at positions not facing each other to coincide with the approximate center of the measurement region,
In the step (c), the approximate center of the sample flow intersects the optical axis of the desired at least one scattering / fluorescence light receiving unit than the approximate center of the measurement region. as through the remote location, the optical information analysis method according to claim 13, characterized in that the relative adjustment of the position of the sample flow in the channel. The optical information analysis according to claim 15 or 16 , wherein in the step (d), the optical axis of the scattering / fluorescent light receiving unit and the optical axis of the irradiation unit are substantially orthogonal within the measurement region. Method. In the step (c), the position of the sample flow is adjusted with respect to the measurement region by a nozzle position adjusting mechanism that adjusts the position of the tip of the introduction nozzle in the flow path of the flow cell. The optical information analysis method according to any one of claims 13 to 17. In the step (c), the tip of the introduced introduction nozzle is adjusted by attaching the introduction nozzle and fixing the tip to the flow cell to adjust the position of the tip of the introduction nozzle in the flow path of the flow cell. By the optimal offset jig selected from a plurality of offset jigs having different positions, the position of the introduction nozzle in the flow path is set to a desired position of the sample flow with respect to the measurement region. the optical information analyzing method according to any one of claims 13 to 17, characterized in that to adjust the position of the tip.

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